Canonical Allele Identifier: PA916047728
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Arg13Leu
CA270350
NM_001369394.2:c.38G>T